Semiconducting polymer

ABSTRACT

Compounds of formula (I) and polymers comprising at least a structure of formula (II), wherein T 1  or T 2  are independently of each other a group of Formula (III), Formula (iv) Q a , Q b , Q c , Q d , Q e  or Q f  are independently of each other O, S or NR 1 .

The present invention relates to polymers, to a process for the preparation of these polymers, to intermediates, to electronic devices comprising these polymers, as well as to the use of these polymers as semiconducting material.

Organic semiconducting materials can be used in electronic devices such as organic photovoltaic devices (OPVs), organic field-effect transistors (OFETs), organic light emitting diodes (OLEDs), organic photodiodes (OPDs) and organic electrochromic devices (ECDs).

It is desirable that the organic semiconducting materials are compatible with liquid processing techniques such as spin coating as liquid processing techniques are convenient from the point of processability, and thus allow the production of low cost organic semiconducting material-based electronic devices. In addition, liquid processing techniques are also compatible with plastic substrates, and thus allow the production of light weight and mechanically flexible organic semiconducting material-based electronic devices.

For application in organic photovoltaic devices (OPVs), organic field-effect transistors (OFETs), and organic photodiodes (OPDs), it is further desirable that the organic semiconducting materials show high charge carrier mobility.

For application in organic photovoltaic devices (OPVs) and organic photodiodes (OPDs), the organic semiconducting materials should also show a strong absorption of the visible light and of the near infra-red light.

G. Kossmehl and G. Manecke, Die Makromolekulare Chemie 176 (1975), pp. 333-340 discloses the following structures

which have coplanar conjugated π-electron systems.

WO 2009/053291 describes semiconducting polymers comprising the following units

and organic field effect transistors comprising these polymers.

WO 2014/071524 discloses monomers, oligomers and polymers comprising a fused ring moiety of the following structure

where X is independently O, S or NR and R is independently hydrogen, or an optionally substituted hydrocarbon.

WO 2016/005891 discloses polymers comprising at least one unit of formulae

as semiconducting materials for electronic devices.

It was the object of the present invention to provide organic semiconducting materials.

It was a second object of the present invention to provide semiconducting polymers which can be synthesized without the need of noble metal catalysts.

The problem is solved by compounds of formula (I)

and polymers comprising at least a structure of formula (II)

and preferably polymers comprising at least a structure of formula (II′)

wherein n is 3 to 1000, T¹ or T² are independently of each other a group of formulae ═O, ═S, ═NR^(1a), ═CR⁴R^(4′),

Q^(a), Q^(b), Q^(c), Q^(d), Q^(e) or Q^(f) are independently of each other O, S or NR¹, preferably O or NR¹, Hal is halogen, preferably Cl or Br, especially Cl.

T¹ or T² are preferably independently of each other a group of formulae ═O, ═CR⁴R^(4′),

T¹ or T² are more preferably independently of each other a group of formulae

T¹ or T² are even more preferably independently of each other a group of formulae

T¹ or T² are most preferably independently of each other a group of formula;

The polymers comprising a structure of formula (II) or (II′) can be linked to other moieties by double bonds, e.g. to other groups of formula (II) or (II′), or e.g. to end groups T¹ or T².

Ar, Ar′, Ar^(e) and Ar^(f) are independently of each other a 5- to 6-membered ring, or a ring system comprising from 2 to 6 fused 5- to 6-membered rings, wherein at least one of the rings is an aromatic or heteroaromatic ring.

Ar and Ar′ are preferably independently of each other selected from the group consisting of

wherein Ar or Ar′ is bound via the single bonds

and

to the moieties

wherein Q is O, S or NR¹, preferably O or NR¹, Ar and Ar′ are more preferably independently of each other selected from the group consisting of

wherein Ar or Ar′ is bound via the single bonds

and

to the moieties

wherein Q is O, S or NR¹, preferably O or NR¹, Ar and Ar′ are even more preferably independently of each other selected from

Ar and Ar′ are most preferably independently of each other selected from

Ar^(e) is preferably selected from

where Ar^(e) is bound via the bonds

and

to the moiety

Ar^(e) is more preferably selected from

Ar^(e) is even more preferably selected from

Ar^(e) is most preferably

Ar^(f) is preferably selected from the group consisting of

Ar^(f) is more preferably selected from

Ar^(f) is most preferably selected from

wherein Ar, Ar′, Ar^(e), Ar^(f) can be substituted by one or more substituents R².

Y, Y′, Y″ and Y* are at each occurrence O, S, NR^(1a), Se, Te, preferably O, S, NR^(1a), Se, more preferably O, S, Se, still more preferably S, Se and most preferably S.

R^(W) is at each occurrence H, C₁₋₃₀-alkyl, C₁₋₃₀-alkoxy, or a moiety

preferably H, C₁₋₃₀-alkyl, or C₁₋₃₀-alkoxy, more preferably H or C₁₋₃₀-alkoxy, most preferably H, wherein R^(s1), R^(s2), R^(s3) are independently of each other H, C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl, or phenyl, preferably C₁₋₂₀-alkyl.

R¹, R^(1a) are at each occurrence selected from the group consisting of H, C₁₋₁₀₀-alkyl, C₂₋₁₀₀-alkenyl, C₂₋₁₀₀-alkynyl, C₅₋₁₂-cycloalkyl, C₆₋₁₈-aryl, a 5 to 20 membered heteroaryl, C(O)—C₁₋₁₀₀-alkyl, C(O)—C₅₋₁₂-cycloalkyl and C(O)—OC₁₋₁₀₀-alkyl,

-   wherein -   C₁₋₁₀₀-alkyl, C₂₋₁₀₀-alkenyl and C₂₋₁₀₀-alkynyl can be substituted     with one to forty substituents independently selected from the group     consisting of C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5 to 14 membered     heteroaryl, OR^(a), OC(O)—R^(a), C(O)—OR^(a), C(O)—R^(a),     NR^(a)R^(b), NR^(a)—C(O)R^(b), C(O)NR^(a)R^(b),     N[C(O)R^(a)][C(O)R^(b)], SR^(a), Si(R^(Sia))(R^(Sib))(R^(Sic)),     —O—Si(R^(Sia))(R^(Sib))(R^(Sic)), halogen, CN, and NO₂; and at least     two CH₂-groups, but not adjacent CH₂-groups, of C₁₋₁₀₀-alkyl,     C₂₋₁₀₀-alkenyl and C₂₋₁₀₀-alkynyl can be replaced by O or S, -   C₅₋₁₂-cycloalkyl can be substituted with one to six substituents     independently selected from the group consisting of C₁₋₆₀-alkyl,     C₂₋₆₀-alkenyl, C₂₋₆₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5 to 14     membered heteroaryl, OR^(a), OC(O)—R^(a), C(O)—OR^(a), C(O)—R^(a),     NR^(a)R^(b), NR^(a)—C(O)R^(b), C(O)—NR^(a)R^(b),     N[C(O)R^(a)][C(O)R^(b)], SR^(a), Si(R^(Sia))(R^(Sib))(R^(Sic)),     —O—Si(R^(Sia))(R^(Sib))(R^(Sic)), halogen, CN, and NO₂; and one or     two CH₂-groups, but not adjacent CH₂-groups, of C₅₋₁₂-cycloalkyl can     be replaced by O, S, OC(O), CO, NR^(a) or NR^(a)—CO, -   C₆₋₁₈-aryl and 5 to 20 membered heteroaryl can be substituted with     one to six substituents independently selected from the group     consisting of C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl, C₂₋₆₀-alkynyl,     C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5 to 14 membered heteroaryl, OR^(a),     OC(O)—R^(a), C(O)—OR^(a), C(O)R^(a), NR^(a)R^(b), NR^(a)—C(O)R^(b),     C(O)—NR^(a)R^(b), N[C(O)R^(a)][C(O)R^(b)], SR^(a),     Si(R^(Sia))(R^(Sib))(R^(Sic)), —O—Si(R^(Sia))(R^(Sib))(R^(Sic)),     halogen, CN, and NO₂,     -   wherein     -   R^(a) and R^(b) are independently selected from the group         consisting of H, C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl, C₂₋₆₀-alkynyl,         C₅₋₈-cycloalkyl, C₆₋₁₄-aryl and 5 to 14 membered heteroaryl,     -   R^(Sia), R^(Sib) and R^(Sic) are independently selected from the         group consisting of H, C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl,         C₂₋₆₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5 to 14 membered         heteroaryl, O—C₁₋₆₀-alkyl, O—C₂₋₆₀-alkenyl, O—C₂₋₆₀-alkynyl,         O—C₅₋₈-cycloalkyl, O—C₆₋₁₄-aryl, O-5 to 14 membered heteroaryl,         —[O—SiR^(Sid)R^(Sie)]_(o)—R^(Sif), NR⁵R⁶, halogen and O—C(O)—R⁵,         -   wherein         -   o is an integer from 1 to 50,         -   R^(Sid), R^(Sie), R^(Sif) are independently selected from             the group consisting of H, C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl,             C₂₋₆₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5 to 14 membered             heteroaryl, O—C₁₋₆₀-alkyl, O—C₂₋₆₀-alkenyl, O—C₂₋₆₀-alkynyl,             O—C₅₋₈-cycloalkyl, O—C₆₋₁₄-aryl, O-5 to 14 membered             heteroaryl, —[O—SiR^(Sig)R^(Sih)]_(p)—R^(Sii), NR⁵⁰R⁶⁰,             halogen and O—C(O)—R⁵⁰;             -   wherein             -   p is an integer from 1 to 50,             -   R^(Sig) R^(Sih), R^(Sii) are independently selected from                 the group consisting of H, C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl,                 C₂₋₃₀-alkynyl, C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, 5 to 10                 membered heteroaryl, O—C₁₋₃₀-alkyl, O—C₂₋₃₀-alkenyl,                 O—C₂₋₃₀-alkynyl, O—C₅₋₆-cycloalkyl, OC₆₋₁₀-aryl, O-5 to                 10 membered heteroaryl, O—Si(CH₃)₃, NR⁵⁰⁰R⁶⁰⁰, halogen                 and O—C(O)—R₅₀₀,         -   R⁵, R⁶, R⁵⁰, R⁶⁰, R⁵⁰⁰ and R⁶⁰⁰ are independently selected             from the group consisting of H, C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl,             C₂₋₆₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, and 5 to 14             membered heteroaryl,         -   C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl and C₂₋₆₀-alkynyl can be             substituted with one to twenty substituents selected from             the group consisting of C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, OR^(c),             OC(O)—R^(c), C(O)—OR^(c), C(O)—R^(c), NR^(c)R^(d),             NR^(c)—C(O)R^(d), C(O)—NR^(c)R^(d), N[C(O)R^(c)][C(O)R^(d)],             SR^(c), Si(R^(Sij))(R^(Sik))(R^(Sil)),             —O—Si(R^(Sij))(R^(Sik))(R^(Sil)), halogen, CN, and NO₂; and             at least two CH₂-groups, but not adjacent CH₂-groups, of             C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl and C₂₋₆₀-alkynyl can be replaced             by O or S,         -   C₅₋₈-cycloalkyl can be substituted with one to five             substituents selected from the group consisting of             C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₅₋₆-cycloalkyl,             C₆₋₁₀-aryl, OR^(c), OC(O)—R^(c), C(O)—OR^(c), C(O)—R^(c),             NR^(c)R^(d), NR^(c)—C(O)R^(d), C(O)—NR^(c)R^(d),             N[C(O)R^(c)][C(O)R^(d)], SR^(c),             Si(R^(Sij))(R^(Sik))(R^(Sil)),             —O—Si(R^(Sij))(R^(Sik))(R^(Sil)), halogen, CN, and NO₂; and             one or two CH₂-groups, but not adjacent CH₂-groups, of             C₅₋₈-cycloalkyl can be replaced by O, S, OC(O), CO, NR^(c)             or NR^(c)—CO,         -   C₆₋₁₄-aryl and 5 to 14 membered heteroaryl can be             substituted with one to five substituents independently             selected from the group consisting of C₁₋₃₀-alkyl,             C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₅₋₆-cycloalkyl, C₆₋₁₀-aryl,             OR^(c), OC(O)—R^(c), C(O)—OR^(c), C(O)—R^(c), NR^(c)R^(d),             NR^(c)—C(O)R^(d), C(O)—NR^(c)R^(d), N[C(O)R^(c)][C(O)R^(d)],             SR^(c), Si(R^(Sij))(R^(Sik))(R^(Sil)),             —O—Si(R^(Sij))(R^(Sik))(R^(Sil)), halogen, CN and NO₂,             -   wherein             -   R^(c) and R^(d) are independently selected from the                 group consisting of H, C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl and                 C₂₋₃₀-alkynyl,             -   R^(Sij), R^(Sik) and R^(Sil) are independently selected                 from the group consisting of H, C₁₋₃₀-alkyl,                 C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₅₋₆-cycloalkyl,                 C₆₋₁₀-aryl, 5 to 10 membered heteroaryl, O—C₁₋₃₀-alkyl,                 O—C₂₋₃₀-alkenyl, O—C₂₋₃₀-alkynyl, O—C₅₋₆-cycloalkyl,                 O—C₆₋₁₀-aryl, O-5 to 10 membered heteroaryl,                 —[O—SiR^(Sim)R^(Sin)]_(q)—R^(Sio), NR⁷R⁸, halogen, and                 O—C(O)—R⁷,                 -   wherein                 -   q is an integer from 1 to 50,                 -   R^(Sim), R^(Sin), R^(Sio) are independently selected                     from the group consisting of H, C₁₋₃₀-alkyl,                     C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₅₋₆-cycloalkyl,                     C₆₋₁₀-aryl, 5 to 10 membered heteroaryl,                     O—C₁₋₃₀-alkyl, O—C₂₋₃₀-alkenyl, O—C₂₋₃₀-alkynyl,                     O—C₅₋₆-cycloalkyl, O—C₆₋₁₀-aryl, O-5 to 10 membered                     heteroaryl, —[O—SiR^(Sip)R^(Siq)]_(r)—R^(Sir),                     NR⁷⁰R⁸⁰, halogen, and O—C(O)—R⁷⁰,                 -    wherein                 -    r is an integer from 1 to 50,                 -    R^(Sip), R^(Siq), R^(Sir) are independently                     selected from the group consisting of H,                     C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl,                     C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, 5 to 10 membered                     heteroaryl, O—C₁₋₃₀-alkyl, O—C₂₋₃₀-alkenyl,                     O—C₂₋₃₀-alkynyl, O—C₅₋₆-cycloalkyl, O—C₆₋₁₀-aryl,                     O-5 to 10 membered heteroaryl, O—Si(CH₃)₃,                     NR⁷⁰⁰R⁸⁰⁰, halogen and O—C(O)—R⁷⁰⁰,                 -   R⁷, R⁸, R⁷⁰, R⁸⁰, R⁷⁰⁰ and R⁸⁰⁰ are independently                     selected from the group consisting of H,                     C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl,                     C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, and 5 to 10 membered                     heteroaryl,             -   C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl and C₂₋₃₀-alkynyl can be                 substituted with one to ten substituents selected from                 the group consisting of halogen, CN and NO₂. -   R¹, R^(1a) are preferably at each occurrence selected from the group     consisting of H, C₁₋₁₀₀-alkyl, C₃₋₁₀₀-alkenyl, C₃₋₁₀₀-alkynyl,     -   wherein     -   C₁₋₁₀₀-alkyl, C₃₋₁₀₀-alkenyl and C₃₋₁₀₀-alkynyl can be         substituted with one to forty substituents independently         selected from the group consisting of C₅₋₈-cycloalkyl, OR^(a),         OC(O)—R^(a), C(O)—OR^(a), C(O)—R^(a),         Si(R^(Sia))(R^(Sib))(R^(Sic)), and halogen; and at least two         CH₂-groups, but not adjacent CH₂-groups, of C₁₋₁₀₀-alkyl,         C₃₋₁₀₀-alkenyl and C₃₋₁₀₀-alkynyl can be replaced by O or S,         -   wherein         -   R^(a) is selected from the group consisting of H,             C₁₋₆₀-alkyl, C₃₋₆₀-alkenyl, C₃₋₆₀-alkynyl, C₅₋₈-cycloalkyl,         -   R^(Sia), R^(Sib) and R^(Sic) are independently selected from             the group consisting of H, C₁₋₆₀-alkyl, C₂₋₆₀-alkenyl,             C₂₋₆₀-alkynyl, C₅₋₈-cycloalkyl, —[O—Si             R^(Sid)R^(Sie)]_(o)—R^(Sif),             -   wherein             -   o is an integer from 1 to 50,             -   R^(Sid), R^(Sie), R^(Sif) are independently selected                 from the group consisting of H, C₁₋₆₀-alkyl,                 C₂₋₆₀-alkenyl, C₂₋₆₀-alkynyl, C₅₋₈-cycloalkyl and                 —[O—SiR^(Sig)R^(Sih)]_(p)—R^(Sii);                 -   wherein                 -   p is an integer from 1 to 50,                 -   R^(Sig) R^(Sih), R^(Sii) are independently selected                     from the group consisting of H, C₁₋₃₀-alkyl,                     C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₅₋₆-cycloalkyl,                     O—Si(CH₃)₃, -   R¹, R^(1a) are more preferably at each occurrence selected from the     group consisting of H, C₁₋₅₀-alkyl, C₃₋₅₀-alkenyl, C₃₋₅₀-alkynyl,     -   wherein     -   C₁₋₅₀-alkyl, C₃₋₅₀-alkenyl and C₃₋₅₀-alkynyl can be substituted         with one to twenty substituents independently selected from the         group consisting of OR^(a), OC(O)—R^(a), C(O)—OR^(a),         Si(R^(Sia))(R^(Sib))(R^(Sic)), and halogen; and at least two         CH₂-groups, but not adjacent CH₂-groups, of C₁₋₅₀-alkyl,         C₃₋₅₀-alkenyl and C₃₋₅₀-alkynyl can be replaced by O or S,         -   wherein         -   R^(a) is selected from the group consisting of H,             C₁₋₂₀-alkyl, C₃₋₂₀-alkenyl, C₃₋₂₀-alkynyl,         -   R^(Sia), R^(Sib) and R^(Sic) are independently selected from             the group consisting of H, C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl,             —[O—SiR^(Sid)R^(Sie)]_(o)—R^(Sif),             -   wherein             -   o is an integer from 1 to 20,             -   R^(Sid), R^(Sie), R^(Sif) are independently selected                 from the group consisting of H, C₁₋₂₀-alkyl,                 C₂₋₂₀-alkenyl, and —[O—SiR^(Sig)R^(Sih)]_(p)—R^(Sii);                 -   wherein                 -   p is an integer from 1 to 20,                 -   R^(Sig) R^(Sih), R^(Sii) are independently selected                     from the group consisting of H, C₁₋₂₀-alkyl,                     C₂₋₂₀-alkenyl, O—Si(CH₃)₃, -   R¹, R^(1a) are even more preferably at each occurrence selected from     the group consisting of C₁₋₅₀-alkyl, C₃₋₅₀-alkenyl, C₃₋₅₀-alkynyl,     -   wherein     -   C₁₋₅₀-alkyl, C₃₋₅₀-alkenyl and C₃₋₅₀-alkynyl can be substituted         with one to twenty substituents independently selected from the         group consisting of OR^(a), and halogen; and at least two         CH₂-groups, but not adjacent CH₂-groups, of C₁₋₅₀-alkyl,         C₃₋₅₀-alkenyl and C₃₋₅₀-alkynyl can be replaced by O or S,         -   wherein         -   R^(a) is selected from the group consisting of H,             C₁₋₂₀-alkyl, C₃₋₂₀-alkenyl, C₃₋₂₀-alkynyl, -   R¹, R^(1a) are much more preferably at each occurrence selected from     the group consisting of C₁₋₅₀-alkyl,     -   wherein     -   C₁₋₅₀-alkyl can be substituted with one to twenty substituents         independently selected from the group consisting of OR^(a), and         halogen; and at least two CH₂-groups, but not adjacent         CH₂-groups, of C₁₋₅₀-alkyl can be replaced by O or S,         -   wherein         -   R^(a) is selected from the group consisting of H, or             C₁₋₂₀-alkyl, -   R¹, R^(1a) are especially preferably at each occurrence selected     from the group consisting of C₁₋₅₀-alkyl,     -   wherein     -   C₁₋₅₀-alkyl can be substituted with one to twenty halogens; -   R¹, R^(1a) are most preferably C₁₋₅₀-alkyl,     -   R² is at each occurrence selected from the group consisting of         C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₅₋₁₂-cycloalkyl,         C₆₋₁₈-aryl, 5 to 20 membered heteroaryl, OR²¹, OC(O)—R²¹,         C(O)OR²¹, C(O)—R²¹, NR²¹R²², NR²¹—C(O)R²², C(O)—NR²¹R²²,         N[C(O)R²¹][C(O)R²²], SR²¹, halogen, CN, SiR^(Sis)R^(Sit)R^(Siu)         and OH,         -   wherein         -   R²¹ and R²² and are independently selected from the group             consisting of H, C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl,             C₅₋₁₂-cycloalkyl, C₆₋₁₈-aryl and 5 to 20 membered             heteroaryl, and         -   C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl and C₂₋₃₀-alkynyl can be             substituted with one to ten substituents independently             selected from the group consisting of C₅₋₈-cycloalkyl,             C₆₋₁₄-aryl, 5 to 14 membered heteroaryl, OR^(e),             OC(O)—R^(e), C(O)—OR^(e), C(O)—R^(e), NR^(e)R^(f),             NR^(e)—C(O)R^(f), C(O)NR^(e)R^(f), N[C(O)R^(e)][C(O)R^(f)],             SR^(e), halogen, CN, SiR^(Sis)R^(Sit)R^(Siu) and NO₂; and at             least two CH₂-groups, but not adjacent CH₂-groups, of             C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl and C₂₋₃₀-alkynyl can be replaced             by O or S,         -   C₅₋₁₂-cycloalkyl can be substituted with one to six             substituents independently selected from the group             consisting of C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl and C₂₋₂₀-alkynyl,             C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5 to 14 membered heteroaryl,             OR^(e), OC(O)—R^(e), C(O)—OR^(e), C(O)—R^(e), NR^(e)R^(f),             NR^(e)—C(O)R^(f), C(O)—NR^(e)R^(f), N[C(O)R^(e)][C(O)R^(f)],             SR^(e), halogen, CN, SiR^(Sis)R^(Sit)R^(Siu) and NO₂; and             one or two CH₂-groups, but not adjacent CH₂-groups, of             C₅₋₁₂-cycloalkyl can be replaced by O, S, OC(O), CO, NR^(e)             or NR^(e)—CO,         -   C₆₋₁₈-aryl and 5 to 20 membered heteroaryl can be             substituted with one to six substituents independently             selected from the group consisting of C₁₋₂₀-alkyl,             C₂₋₂₀-alkenyl, C₂₋₂₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5             to 14 membered heteroaryl, OR^(e), OC(O)—R^(e), C(O)—OR^(e),             C(O)R^(e), NR^(e)R^(f), NR^(e)—C(O)R^(f), C(O)—NR^(e)R^(f),             N[C(O)R^(e)][C(O)R^(f)], SR^(e), halogen, CN,             SiR^(Sis)R^(Sit)R^(Siu) and NO₂,         -   wherein             -   R^(Sis), R^(Sit) and R^(Siu) are independently from each                 other selected from the group consisting of H,                 C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl, C₂₋₂₀-alkynyl,                 C₅₋₆-cycloalkyl, phenyl and O—Si(CH₃)₃,             -   R^(e) and R^(f) are independently selected from the                 group consisting of H, C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl,                 C₂₋₂₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, and 5 to 14                 membered heteroaryl,                 -   wherein                 -   C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl and C₂₋₂₀-alkynyl can be                     substituted with one to five substituents selected                     from the group consisting of C₅₋₆-cycloalkyl,                     C₆₋₁₀-aryl, 5 to 10 membered heteroaryl, OR^(g),                     OC(O)—R^(g), C(O)—OR^(g), C(O)—R^(g), NR^(g)R^(h),                     NR^(g)—C(O)R^(h), C(O)NR^(g)R^(h),                     N[C(O)R^(g)][C(O)R^(h)], SR^(g), halogen, CN, and                     NO₂,                 -   C₅₋₈-cycloalkyl can be substituted with one to five                     substituents selected from the group consisting of                     C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl, C₂₋₁₀-alkynyl,                     C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, 5 to 10 membered                     heteroaryl, OR^(g), OC(O)—R^(g), C(O)—OR^(g),                     C(O)—R^(g), NR^(g)R^(h), NR^(g)C(O)R^(h),                     C(O)—NR^(g)R^(h), N[C(O)R^(g)][C(O)R^(h)], SR^(g),                     halogen, CN, and NO₂,                 -   C₆₋₁₄-aryl and 5 to 14 membered heteroaryl can be                     substituted with one to five substituents                     independently selected from the group consisting of                     C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl, C₂₋₁₀-alkynyl,                     C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, 5 to 10 membered                     heteroaryl, OR^(g), OC(O)—R^(g), C(O)—OR^(g),                     C(O)—R^(g), NR^(g)R^(h), NR^(g)—C(O)R^(h),                     C(O)—NR^(g)R^(h), N[C(O)R^(g)][C(O)R^(h)], SR^(g),                     halogen, CN, and NO₂,                 -    wherein                 -    R^(g) and R^(h) are independently selected from the                     group consisting of H, C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl                     and C₂₋₁₀-alkynyl,                 -    wherein                 -    C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl and C₂₋₁₀-alkynyl can be                     substituted with one to five substituents selected                     from the group consisting of halogen, CN and NO₂.     -   R² is preferably at each occurrence selected from the group         consisting of C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, OR²¹,         C(O)—OR²¹, C(O)—R²¹, halogen, and CN,         -   wherein         -   R²¹ is selected from the group consisting of H, C₁₋₃₀-alkyl,             C₃₋₃₀-alkenyl, C₃₋₃₀-alkynyl, and         -   C₁₋₃₀-alkyl, C₃₋₃₀-alkenyl and C₃₋₃₀-alkynyl can be             substituted with one to ten substituents independently             selected from the group consisting of OR^(e), OC(O)—R^(e),             C(O)—OR^(e), C(O)—R^(e), and halogen; and at least two             CH₂-groups, but not adjacent CH₂-groups, of C₁₋₃₀-alkyl,             C₃₋₃₀-alkenyl and C₃₋₃₀-alkynyl can be replaced by O or S,         -   wherein             -   R^(e) is selected from the group consisting of H,                 C₁₋₂₀-alkyl, C₃₋₂₀-alkenyl, C₃₋₂₀-alkynyl.     -   R² is more preferably at each occurrence selected from the group         consisting of C₁₋₃₀-alkyl, OR²¹, and halogen,         -   wherein         -   R²¹ is C₁₋₃₀-alkyl, and         -   C₁₋₃₀-alkyl can be substituted with one to ten substituents             independently selected from the group consisting of OR^(e),             and halogen; and at least two CH₂-groups, but not adjacent             CH₂-groups, of C₁₋₃₀-alkyl can be replaced by O or S,         -   wherein R^(e) is independently selected from the group             consisting of H, or C₁₋₂₀-alkyl.     -   R² is even more preferably at each occurrence selected from the         group consisting of C₁₋₂₀-alkyl, OR²¹, and halogen,         -   wherein R²¹ is C₁₋₂₀-alkyl, and         -   C₁₋₂₀-alkyl can be substituted with one to ten halogens; and             at least two CH₂-groups, but not adjacent CH₂-groups, of             C₁₋₂₀-alkyl can be replaced by O or S.     -   R² is much more preferably at each occurrence selected from the         group consisting of C₁₋₂₀-alkyl, OR²¹, and halogen,         -   wherein         -   R²¹ is C₁₋₂₀-alkyl, which can optionally be substituted with             one to ten halogens.     -   R² is especially preferably at each occurrence selected from the         group consisting of C₁₋₂₀-alkyl, OR²¹, and halogen,         -   wherein         -   R²¹ is C₁₋₂₀-alkyl.     -   R² is most preferably at each occurrence selected from the group         consisting of OR²¹, and halogen,         -   wherein R²¹ is C₁₋₂₀-alkyl.     -   R⁴ and R^(4′) are independently and at each occurrence selected         from the group consisting of H, C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl,         C₂₋₃₀-alkynyl, C₅₋₁₂-cycloalkyl, C₆₋₁₈-aryl and 5 to 20 membered         heteroaryl, C(O)—R⁴¹, C(O)—NR⁴¹R⁴², C(O)—OR⁴¹ and CN,         -   wherein         -   R⁴¹ und R⁴² are independently from each other and at each             occurrence selected from the group consisting of H,             C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₅₋₁₂-cycloalkyl,             C₆₋₁₈-aryl and 5 to 20 membered heteroaryl, and         -   wherein         -   C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl and C₂₋₃₀-alkynyl can be             substituted with one to ten substituents independently             selected from the group consisting of C₅₋₈-cycloalkyl,             C₆₋₁₄-aryl, 5 to 14 membered heteroaryl, OR^(i),             OC(O)—R^(j), C(O)—OR^(i), C(O)—R^(i), NR^(i)R^(j),             NR^(i)—C(O)R^(j), C(O)—NR^(i)R^(j), N[C(O)R^(i)][C(O)R^(j)],             SR^(i), halogen, CN, and NO₂; and at least two CH₂-groups,             but not adjacent CH₂-groups of C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl             and C₂₋₃₀-alkynyl can be replaced by O or S,         -   C₅₋₁₂-cycloalkyl can be substituted with one to six             substituents independently selected from the group             consisting of C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl and C₂₋₂₀-alkynyl,             C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5 to 14 membered heteroaryl,             OR^(i), OC(O)—R^(j), C(O)—OR^(i), C(O)—R^(i), NR^(i)R^(j),             NR^(i)—C(O)R^(j), C(O)—NR^(i)R^(j), N[C(O)R^(i)][C(O)R^(j)],             SR^(i), halogen, CN, and NO₂; and one or two CH₂-groups, but             not adjacent CH₂-groups, of C₅₋₁₂-cycloalkyl can be replaced             by O, S, OC(O), CO, NR^(i) or NR^(i)—CO,         -   C₆₋₁₈-aryl and 5 to 20 membered heteroaryl can be             substituted with one to six substituents independently             selected from the group consisting of C₁₋₂₀-alkyl,             C₂₋₂₀-alkenyl, C₂₋₂₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, 5             to 14 membered heteroaryl, OR^(i), OC(O)—R^(j), C(O)—OR^(i),             C(O)—R^(i), NR^(i)R^(j), NR^(i)—C(O)R^(j), C(O)—NR^(i)R^(j),             N[C(O)R^(i)][C(O)R^(j)], SR^(i), halogen, CN, and NO₂,             -   Ri and Rj are independently selected from the group                 consisting of H, C₁₋₂₀-alkyl, 20 C₂₋₂₀-alkenyl,                 C₂₋₂₀-alkynyl, C₅₋₈-cycloalkyl,     -   R⁴ and R^(4′) are preferably independently and at each         occurrence selected from the group consisting of H, C₁₋₃₀-alkyl,         C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, C₆₋₁₈-aryl and 5 to 20 membered         heteroaryl, C(O)—R⁴¹, C(O)—NR⁴¹R⁴², C(O)—OR⁴¹ and CN,         -   wherein         -   R⁴¹ und R⁴² are independently from each other and at each             occurrence selected from the group consisting of H,             C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl, and         -   wherein         -   C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl and C₂₋₃₀-alkynyl can be             substituted with one to ten substituents independently             selected from the group consisting of OR^(i), and halogen;             and at least two CH₂-groups, but not adjacent CH₂-groups of             C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl and C₂₋₃₀-alkynyl can be replaced             by O or S,         -   C₆₋₁₈-aryl and 5 to 20 membered heteroaryl can be             substituted with one to six substituents independently             selected from the group consisting of C₁₋₂₀-alkyl, OR^(i),             halogen,             -   Ri is selected from the group consisting of H,                 C₁₋₂₀-alkyl,             -   20 C₂₋₂₀-alkenyl, C₂₋₂₀-alkynyl, C₅₋₈-cycloalkyl,     -   R⁴ and R^(4′) are more preferably independently and at each         occurrence selected from the group consisting of H, C₁₋₃₀-alkyl,         C(O)—R⁴¹, C(O)—NR⁴¹R⁴², C(O)—OR⁴¹ and CN,         -   wherein         -   R⁴¹ und R⁴² are independently from each other and at each             occurrence selected from the group consisting of H, or             C₁₋₃₀-alkyl,     -   R⁴ and R^(4′) are most preferably independently and at each         occurrence selected from the group consisting of C(O)—R⁴¹,         C(O)—NR⁴¹R⁴², C(O)—OR⁴¹ and CN,         -   wherein         -   R⁴¹ und R⁴² are independently from each other and at each             occurrence selected from the group consisting of H, or             C₁₋₃₀-alkyl, -   R²⁰⁰ is hydrogen, C₁-C₃₆alkyl, C₂-C₃₆alkenyl, C₂-C₃₆alkinyl, Ar²⁰⁰,     CN, COOR²⁰¹, CONR²⁰²R²⁰³, COR²⁰⁴. -   R²⁰¹, R²⁰², R²⁰³ and R²⁰⁴ are independently of each other hydrogen,     C₁-C₃₆alkyl, C₂-C₃₆alkenyl, C₂-C₃₆alkinyl, or phenyl; -   Ar²⁰⁰ has the meaning of Ar^(f); -   Halogen can be F, Cl, Br and I.

C₁₋₄-alkyl, C₁₋₁₀-alkyl, C₁₋₂₀-alkyl, C₁₋₃₀-alkyl, C₁₋₃₆-alkyl, C₁₋₅₀-alkyl, C₁₋₆₀-alkyl and C₁₋₁₀₀-alkyl can be branched or unbranched. Examples of C₁₋₄-alkyl are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl and tert-butyl. Examples of C₁₋₁₀-alkyl are C₁₋₄-alkyl, n-pentyl, neopentyl, isopentyl, n-(1-ethyl)propyl, n-hexyl, n-heptyl, n-octyl, n-(2-ethyl)hexyl, n-nonyl and n-decyl. Examples of C₁₋₂₀-alkyl are C₁₋₁₀-alkyl and n-undecyl, n-dodecyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-icosyl (C₂₀). Examples of C₁₋₃₀-alkyl, C₁₋₃₆-alkyl, C₁₋₅₀-alkyl, C₁₋₆₀-alkyl and C₁₋₁₀₀-alkyl are C₁₋₂₀-alkyl and n-docosyl (C₂₂), n-tetracosyl (C₂₄), n-hexacosyl (C₂₆), n-octacosyl (C₂₈) and n-triacontyl (C₃₀).

C₂₋₁₀-alkenyl, C₂₋₂₀-alkenyl, C₂₋₃₀-alkenyl, C₂₋₆₀-alkenyl and C₂₋₁₀₀-alkenyl can be branched or unbranched. Examples of C₁₋₂₀-alkenyl are vinyl, propenyl, cis-2-butenyl, trans-2-butenyl, 3-butenyl, cis-2-pentenyl, trans-2-pentenyl, cis-3-pentenyl, trans-3-pentenyl, 4-pentenyl, 2-methyl-3-butenyl, hexenyl, heptenyl, octenyl, nonenyl and docenyl. Examples of C₂₋₂₀-alkenyl, C₂₋₆₀-alkenyl and C₂₋₁₀₀-alkenyl are C₂₋₁₀-alkenyl and linoleyl (C₁₈), linolenyl (C₁₈), oleyl (C₁₈), and arachidonyl (C₂₀). Examples of C₂₋₃₀-alkenyl are C₂₋₂₀-alkenyl and erucyl (C₂₂).

C₂₋₁₀-alkynyl, C₂₋₂₀-alkynyl, C₂₋₃₀-alkynyl, C₂₋₆₀-alkynyl and C₂₋₁₀₀-alkynyl can be branched or unbranched. Examples of C₂₋₁₀-alkynyl are ethynyl, 2-propynyl, 2-butynyl, 3-butynyl, pentynyl, hexynyl, heptynyl, octynyl, nonynyl and decynyl. Examples of C₂₋₂₀-alkynyl, C₂₋₃₀-alkenyl, C₂₋₆₀-alkynyl and C₂₋₁₀₀-alkynyl are undecynyl, dodecynyl, undecynyl, dodecynyl, tridecynyl, tetradecynyl, pentadecynyl, hexadecynyl, heptadecynyl, octadecynyl, nonadecynyl and icosynyl (C₂₀).

Examples of C₅₋₆-cycloalkyl are cyclopentyl and cyclohexyl. Examples of C₅₋₈-cycloalkyl are C₅₋₆-cycloalkyl and cycloheptyl and cyclooctyl. C₅₋₁₂-cycloalkyl are C₅₋₈-cycloalkyl and cyclononyl, cyclodecyl, cycloundecyl and cyclododecyl.

Examples of C₆₋₁₀-aryl are phenyl,

Examples of C₆₋₁₄-aryl are C₆₋₁₀-aryl and

Examples of C₆₋₁₈-aryl are C₆₋₁₄-aryl and

Preferred aryl moieties are phenyl,

Most preferred is phenyl.

5 to 10 membered heteroaryl are 5 to 10 membered monocyclic or polycyclic, such as dicyclic, tricyclic or tetracyclic, ring systems, which comprise at least one heteroaromatic ring, and which may also comprise non-aromatic rings, which may be substituted by ═O.

5 to 14 membered heteroaryl are 5 to 14 membered monocyclic or polycyclic, such as dicyclic, tricyclic or tetracyclic, ring systems, which comprise at least one heteroaromatic ring, and which may also comprise non-aromatic rings, which may be substituted by ═O.

5 to 20 membered heteroaryl are 5 to 20 membered monocyclic or polycyclic, such as dicyclic, tricyclic or tetracyclic, ring systems, which comprise at least one heteroaromatic ring, and which may also comprise non-aromatic rings, which may be substituted by ═O.

Examples of 5 to 10 membered heteroaryl are

examples of 5 to 14 membered heteroaryl are the examples given for the 5 to 10 membered heteroaryl and

examples of 5 to 20 membered heteroaryl are the examples given for the 5 to 14 membered heteroaryl and

-   -   wherein     -   R¹⁰⁰ and R¹⁰¹ are independently and at each occurrence selected         from the group consisting of H, C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl,         C₂₋₂₀-alkynyl, C₅₋₈-cycloalkyl, C₆₋₁₄-aryl, and 5 to 14 membered         heteroaryl, or R¹⁰⁰ and R¹⁰¹, if attached to the same atom,         together with the atom, to which they are attached, form a 5 to         12 membered ring system,         -   wherein         -   C₁₋₂₀-alkyl, C₂₋₂₀-alkenyl and C₂₋₂₀-alkynyl can be             substituted with one to five substituents selected from the             group consisting of C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, 5 to 10             membered heteroaryl, OR^(q), OC(O)—R^(q), C(O)—OR^(q),             C(O)—R^(q), NR^(q)R^(r), NR^(q)—C(O)R^(r), C(O)—NR^(g)R^(r),             N[C(O)R^(q)][C(O)R^(r)], SR^(q), halogen, CN, and NO₂;         -   C₅₋₈-cycloalkyl can be substituted with one to five             substituents selected from the group consisting of             C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl, C₂₋₁₀-alkynyl, C₅₋₆-cycloalkyl,             C₆₋₁₀-aryl, 5 to 10 membered heteroaryl, OR^(q),             OC(O)—R^(q), C(O)—OR^(q), C(O)—R^(q), NR^(q)R^(r),             NR^(q)—C(O)R^(r), C(O)NR^(q)R^(r), N[C(O)R^(q)][C(O)R^(r)],             SR^(q), halogen, CN, and NO₂;         -   C₆₋₁₄-aryl and 5 to 14 membered heteroaryl can be             substituted with one to five substituents independently             selected from the group consisting of C₁₋₁₀-alkyl,             C₂₋₁₀-alkenyl, C₂₋₁₀-alkynyl, C₅₋₆-cycloalkyl, C₆₋₁₀-aryl, 5             to 10 membered heteroaryl, OR^(q), OC(O)—R^(q), C(O)—OR^(q),             C(O)—R^(q), NR^(q)R^(r), NR^(q)—C(O)R^(r), C(O)—NR^(q)R^(r),             N[C(O)R^(q)][C(O)R^(r)], SR^(q), halogen, CN, and NO₂;         -   5 to 12 membered ring system can be substituted with one to             five substituents selected from the group consisting of             C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl, C₂₋₁₀-alkynyl, C₅₋₆-cycloalkyl,             C₆₋₁₀-aryl, 5 to 10 membered heteroaryl, OR^(q),             OC(O)—R^(q), C(O)—OR^(q), C(O)—R^(q), NR^(q)R^(r),             NR^(q)C(O)R^(r), C(O)—NR^(q)R^(r), N[C(O)R^(q)][C(O)R^(r)],             SR^(q), halogen, CN, and NO₂;             -   wherein             -   R^(q) and R^(r) are independently selected from the                 group consisting of H, C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl and                 C₂₋₁₀-alkynyl,             -   wherein             -   C₁₋₁₀-alkyl, C₂₋₁₀-alkenyl and C₂₋₁₀-alkynyl can be                 substituted with one to five substituents selected from                 the group consisting of halogen, CN and NO₂.

C₆₋₁₈-arylene is a 6 to 18 membered monocyclic or polycyclic, such as dicyclic, tricyclic or tetracyclic, ring system, which comprises at least one C-aromatic ring, and which may also comprise non-aromatic rings, which may be substituted by ═O.

Preferred heteroaryl moieties are

More preferred heteroaryl moieties are

Even more preferred heteroaryl moieties are

Most preferred heteroaryl moiety is

Preferred polymers comprise at least a structure of formula (II′)

where n is an integer of 4 to 500, more preferably n is 5 to 400, more preferably n is 6 to 300, even more preferably n is 7 to 200 and most preferably n is 8 to 100, especially 10 to 50.

Preferably the polymers contain more than 10% by weight groups of formula (II′), more preferably contain more than 30% by weight groups of formula (II′), even more preferably contain more than 50% by weight groups of formula (II′), much more preferably contain more than 70% by weight groups of formula (II′), and most preferably contain more than 90% by weight groups of formula (II′).

Preferred polymers comprise at least one group of formula 1, 2 or 3, wherein groups of formulas 1 and 2 are especially preferred.

More preferably polymers comprise at least one group of formula 1′, 2′ or 3′, wherein groups of formulas 1′ and 2′ are especially preferred and n is defined above or below.

Ar and Ar′ can be the same.

R^(1a) and R^(1b) can be the same.

R^(1c) and R^(1d) can be the same.

R^(1a), R^(1b), R^(1c) and R^(1d) can be the same.

R^(1b), R^(1c) and R^(1d) are defined as R^(1a) above, including the preferred ranges.

The polymers can e.g. be end-capped by moieties T¹ or T².

Very preferred polymers e.g. comprise at least a group

where n is an integer from 3 to 1000 and m is an integer from 3 to 1000.

m is preferably an integer of 4 to 500, more preferably m is 5 to 400, more preferably m is 6 to 300, even more preferably m is 7 to 200 and most preferably m is 8 to 100, especially 10 to 50.

Polymers comprising the formula (II′) can be synthesized e.g. via the following synthesis route 1 by condensation of a tetraone A with a dione B:

In the case of tetraones A, Q^(a) and Q^(b) are preferably substituted nitrogen atoms.

In the case of diones B, Q^(c) and Q^(d) are preferably oxygen or substituted nitrogen atoms.

The condensation can be effected in a solvent like acetic acid, toluene, xylene etc. by the application of heat (room temperature up to reflux temperature of the used solvents). Bases or acids, preferably acids can be added as catalysts.

Such bases can be e.g. sodium acetate and sodium hydroxide.

Such acids can be e.g. protic acids like formic acid, acetic acid, propionic acid, trifluoroacetic acid, HCl, H₂SO₄, HPF₆, para-toluenesulfonic acid, or Lewis acids like AlCl₃, preferably protic acids, especially para-toluenesulfonic acid.

The water obtained by the condensation reaction can be removed e.g. by azeotropic distillation with e.g. toluene as solvent, or e.g. with 4 Å molecular sieves. The ends of these polymers are determined by the starting materials A and B. Special end-cappers might be added during the synthesis like e.g.:

preferably

where R²¹⁰ and R²¹¹ are independently of each other hydrogen, C₁₋₃₀-alkyl, C₂₋₃₀-alkenyl, C₂₋₃₀-alkynyl or C₅₋₁₂-cycloalkyl, preferably C₁₋₃₀-alkyl.

The starting materials A1, A2, B1, B2 wherein Q^(a), Q^(b), Q^(c) and Q^(d) are substituted nitrogen atoms can e.g. be synthesized as follows by synthesis routes 2 or 3:

Synthesis Route 2:

Synthesis Route 3:

Starting materials B where Q^(c) and Q^(d) are oxygen atoms can e.g. be synthesized according to the following methods described in J. Am. Chem. Soc., 1944, 66 (9), pp 1540-1542 for

and Chem. Commun., 2015, 51, 13515-13518 for

Synthesis Route 4

The polymers can be synthesized as well via homo-polymerization of a tetraone A, e.g. by mixing a monomer A with the reagent P(NEt₂)₃ in a solvent, e.g. in toluene:

where m is an integer from 3 to 1000.

The invention also relates to electronic devices comprising the compounds or the polymers of the invention, especially organic field effect transistors.

The invention is illustrated by the following non-limiting examples.

EXAMPLES

The scheme for the synthetic route to 1,5-bis(2-decyltetradecyl)-5,7-dihydropyrrolo[2,3-f]indole-2,6(1H,3H)-dione and 1,5-bis(2-decyltetradecyl)-1,5-dihydropyrrolo[2,3-f]indole-2,3,6,7-tetraone is shown below.

Example 1 Synthesis of 1-bromo-2-decyltetradecane (1)

Under argon, triphenylphosphine (27.8 g, 70.5 mmol) was suspended in a flask with DCM (47 ml). The mixtures was cooled to 0° C. before 2-decyltetradecan-1-ol (29.8 ml, 105.8 mmol) was introduced. After 5 minutes stirring, N-bromosuccinimide (18.8 g, 105.8 mmol) was added portion wise to the flask. The reaction mixture immediately turned yellow and continued to darken to orange. The reaction was stirred for 16 hours after which the solvent was removed by vacuum evaporation. The brown residue was diluted with petroleum ether and the solution flushed through a silica plug. The filtrate was evaporated to give a clear oil. Yield: 28.7 g, 98%. ¹H NMR (400 MHz, Chloroform-d) δ 3.44 (d, J=4.7 Hz, 2H), 1.66-1.47 (m, 2H), 1.44-1.15 (m, 40H), 0.88 (t, J=6.6 Hz, 7H). ¹³C NMR (101 MHz, CDCl₃) δ 39.72, 39.70, 32.75, 32.10, 29.97, 29.82, 29.77, 29.53, 26.74, 22.86, 14.26.

Example 2 Synthesis of 2-(2-decyltetradecyl)isoindoline-1,3-dione

A solution of 1-bromo-2-decyltetradecane (20.0 g, 48.0 mmol) and potassium phthalimide (9.98 g, 52.8 mmol) in DMF (57.2 ml) was refluxed for 16 hours. The reaction mixture was cooled to room temperature and poured into water. The aqueous phase was extracted with DCM three times. The combined organic phase was washed with 0.2 M KOH, followed by H₂O and NH₄Cl. After drying the organic phase with MgSO₄ and filtering the salt, the solvent was removed under vacuum. The residue was subjected to a silica plug using 10% EtOAc in petroleum ether, the yellow oil (14.4 g, 62%) obtained was used immediately.

Example 3 Synthesis of 2-decyltetradecan-1-amine (2)

51% Hydrazine hydrate in water (5.00 ml, 3.1 mmol) was introduced to a solution of 2-(2-decyltetradecyl)isoindoline-1,3-dione (14.40 g, 29.80 mmol) in methanol (10 ml) and refluxed for 16 hours. After cooling, the solvent was removed under vacuum before DCM and 10% KOH solution was added to the residue. The phases were separated and the aqueous phase further extracted with DCM three times. The combined organic phase was washed with brine, dried over MgSO₄, filtered and the solvent removed under reduced pressure. Pale yellow oil, yield 10.0 g, 94% was obtained. ¹H NMR (400 MHz, Chloroform-d) δ 3.51 (d, J=5.5 Hz, 2H), 1.54-1.38 (m, 1H), 1.37-1.17 (m, 40H), 0.94-0.78 (m, 6H). ¹³C NMR (101 MHz, CDCl₃) δ 150.50, 108.43, 45.34, 41.01, 36.21, 32.06, 31.67, 30.25, 29.82, 29.49, 27.96, 26.92, 22.82, 14.23. MS TOF ES+: calculated 354.4100, [M+H]⁺, C24H51N, found 354.4111.

Example 4 Synthesis of N,N′-bis(2-decyltetradecyl)benzene-1,4-diamine (3)

1,4-Cyclohexanedione (0.6 g, 5.0 mmol) was dissolved in ethanol and 2-decyltetradecan-1-amine added to the solution. Air was bubbled through the reaction mixture for 2 hours before the solvent was removed under reduced pressure. The red residue was purified on basified silica gel using 3% EtOAc in petroleum ether to yield 1.8 g, 46% brown oil. ¹H NMR (400 MHz, Chloroform-d) δ 6.54 (s, 4H), 3.24-2.71 (m, 4H), 1.57 (s, 2H), 1.26 (s, 80H), 0.88 (t, J=6.7 Hz, 12H). 13C NMR (101 MHz, CDCl3) δ 141.18, 114.77, 49.07, 37.95, 32.33, 32.09, 30.25, 29.82, 29.52, 26.90, 22.85, 14.27. MS TOF ES+: calculated 781.8278 [M+H]⁺, C54H104N2, found 781.8269.

Example 5 Synthesis of benzene-1,4-diylbis{[(2-decyltetradecyl)imino]-2-oxoethane-2,1-diyl} diacetate (4)

Triethylamine (0.70 ml, 4.99 mmol) was added to N,N′-bis(2-decyltetradecyl)benzene-1,4-diamine (1.77 g, 2.27 mmol) dissolved in dry DCM (22.70 ml) at O ° C. Acetoxyacetyl chloride (0.54 ml, 4.99 mmol) was injected into the flask drop wise before the reaction was allowed to warm to room temperature and stirred for 16 hours. The reaction was quenched with NaHCO₃ and EtOAc added. The phases were separated and the aqueous phase extracted three times with EtOAc. The combined organic phase was washed with brine dried over MgSO₄, the salts filtered and the solvent removed under pressure to give pale yellow solid, 2.00 g, 96%. 1H NMR (400 MHz, Chloroform-d) δ 7.32 (s, 4H), 4.33 (s, 4H), 3.64 (d, J=7.0 Hz, 4H), 2.12 (s, 6H), 1.53-1.41 (m, 2H), 1.37-1.02 (m, 80H), 0.94-0.79 (m, 12H). 13C NMR (101 MHz, CDCl3) δ 170.61, 166.56, 141.13, 129.79, 61.79, 53.41, 36.25, 32.06, 31.23, 30.15, 29.82, 29.75, 29.50, 26.39, 22.83, 20.65, 14.25. MS TOF LD+: C62H112N2O6 [M+H]⁺ found 980.9.

Example 6 Synthesis of N,N′-benzene-1,4-diylbis[N-(2-decyltetradecyl)-2-hydroxyacetamide] (5)

Benzene-1,4-diylbis{[(2-decyltetradecyl)imino]-2-oxoethane-2,1-diyl} diacetate (3.6 g, 3.7 mmol) in THF (200 ml) and MeOH/water mixture (180 ml, 20 ml). The reaction mixture was stirred in the presence of excess K₂CO₃ at room temperature for 16 hours before the salt was filtered off. The mixture was concentrated under reduced pressure and water and ethyl acetate added to the residue. The phases were separated and the aqueous phase is extracted three times with ethyl acetate. The combined organic phases were washed with brine dried over MgSO₄, filtered and the solvent removed in the rotary evaporator to furnish light yellow, 3.1 g, 94%. ¹H NMR (400 MHz, Chloroform-d) δ 7.24 (s, 4H), 3.76 (s, 4H), 3.70 (d, J=7.1 Hz, 4H), 3.47-3.30 (m, 2H), 1.52-1.37 (m, 2H), 1.36-1.04 (m, 80H), 0.86 (t, J=6.7 Hz, 12H). ¹³C NMR (101 MHz, CDCl₃) δ 171.98, 140.31, 129.69, 60.73, 53.47, 36.21, 32.04, 31.23, 30.11, 29.77, 29.71, 29.47, 26.38, 22.80, 14.22. MS TOF LD+: C58H108N2O4, [M+H]⁺ found 898.00.

Example 7 Synthesis of N,N′-(1,4-phenylene)bis(N-(2-decyltetradecyl)-2-oxoacetamide) (6)

Under argon atmosphere, oxalyl chloride (0.31 ml, 3.89 mmol) was diluted with DCM (4 ml) and cooled to −78° C. A solution of DMSO (0.28 ml) in DCM (4.2 ml) was added to the reaction flask at −78° C. The reaction flask was stirred for 20 minutes before N,N′-benzene-1,4-diylbis[N-(2-decyltetradecyl)-2-hydroxyacetamide] (1.45 g, 1.62 mmol) diluted in 7 ml DCM was injected dropwise into the flask. The reaction mixture turns aqua green. After 1.5 hours at −78° C., trimethylamine (2.26 ml, 16.2 mmol) was added slowly. The reaction was then stirred at −78° C. for 4 hours before it was allowed to warm to room temperature slowly. The reaction was stirred for 16 hours before it was quenched with saturated NaHCO₃ solution. The phases were separated and the aqueous phase extracted three times with DCM. The combined organic phases were dried with MgSO₄, filtered and the solvent removed under vacuum to yield brown oil, 0.61 g, which was used immediately.

Example 8 Synthesis of 1,5-bis(2-decyltetradecyl)-3,7-bis(phenylthio)-5,7-dihydropyrrolo[2,3-f]indole-2,6(1H,3H)-dione (7)

Crude N,N′-(1,4-phenylene)bis(N-(2-decyltetradecyl)-2-oxoacetamide) (1.44 g, 1.61 mmol) was diluted with DCM (6 ml) before thiophenol (0.33 ml, 3.23 mml) was added to flask. The reaction mixture was then stirred for 16 hours at room temperature. Following this, TFAA (2.01 ml, 14.50 mmol) was added slowly to the reaction and stirred for 1 hour 30 minutes, after which, BF₃.Et₂O (0.99 ml, 8.05 mmol) was added to the flask cautiously. Following further stirring for 3 hours, the reaction was cooled to 0° C. before it was quenched with NaHCO₃. The aqueous phase was extracted with DCM three times and the organic phases combined and washed with brine and dried over MgSO₄. The solvent was removed under reduced pressure to furnish red/brown residue as the crude product, which was used without further purification. Yield (1.32 g, 76%) MS (TOF ES+): calculated 1077.8244 C70H112N2O2S2, [M+H]+ found 1077.8278.

Example 9 Synthesis of 1,5-bis(2-decyltetradecyl)-1,5-dihydropyrrolo[2,3-f]indole-2,3,6,7-tetraone (9)

Cerium ammonium nitrate (9.48 g, 17.8 mmol) was added to the solution of 1,5-bis(2-decyltetradecyl)-3,7-bis(phenylthio)-5,7-dihydropyrrolo[2,3-f]indole-2,6(1H,3H)-dione (2.40 g, 2.22 mmol) dissolved in a 6:1 ratio of THF/water (42 ml) mixture. Following 30 minutes stirring at room temperature the reaction mixture takes a deep purple colouration. After 3 hours stirring the reaction mixture was reduced under vacuum. The crude residue was purified by column chromatography at a gradient of 3-10% ethyl acetate in petroleum ether 40-60° C. to furnish the titled compound, yield: 300 mg, 15%. ¹H NMR (400 MHz, Chloroform-d) δ 7.12 (s, ArH, 2H), 3.62 (d, J=7.5 Hz, NCH₂, 4H), 1.84 (d, J=9.9 Hz, CH, 2H), 1.40-1.12 (m, CH₂, 80H), 0.88 (t, J=6.7 Hz, CH₃, 12H). ¹³C NMR (101 MHz, CDCl₃) δ 183.36, 157.15, 147.85, 123.24, 106.99, 77.16, 45.49, 36.15, 32.06, 31.52, 30.12, 29.79, 29.76, 29.69, 29.47, 26.40, 22.82, 14.25. MS TOF LD+: C58H100N2O4, [M+H]⁺ found 890.0.

Example 10 Synthesis of 1,5-bis(2-decyltetradecyl)-5,7-dihydropyrrolo[2,3-f]indole-2,6(1H,3H)-dione (8)

1,5-bis(2-decyltetradecyl)-3,7-bis(phenylthio)-5,7-dihydropyrrolo[2,3-f]indole-2,6(1H,3H)-dione was dissolved in dry THF (37.0 ml) and 0.1 M SmI₂ in THF (40.0 ml, 4.0 mol) added to the solution at room temperature. Following 16 hours, saturated NaHCO₃ (200 ml) was introduced into the reaction mixture and the aqueous phase extracted with ethyl acetate three times. The organic layer was washed with brine, dried over MgSO₄, filtered and the solvent removed under reduced pressure. Purification by column chromatography in 15% ethyl acetate in 40-60° C. petroleum ether afforded 800 mg beige solid; yield: 28%. 1H NMR (400 MHz, Chloroform-d) δ 6.73 (s, 2H), 3.56 (d, J=7.9 Hz, ArH 4H), 3.54 (s, CH₂, 4H), 1.91-1.76 (m, CH, 2H), 1.24 (s, CH₂, 80H), 0.87 (t, CH₃, J=6.7 Hz, 12H). ¹³C NMR (101 MHz, CDCl₃) δ 174.85, 140.24, 123.92, 106.05, 44.85, 36.41, 36.25, 32.06, 31.68, 30.20, 29.81, 29.49, 26.60, 22.83, 14.26. MS TOF LD+: C58H104N2O2 [M+H]⁺ found 860.9.

Example 11 Polymerization to Give pDPID P1

A microwave vial was charged with 1,5-bis(2-decyltetradecyl)-5,7-dihydropyrrolo[2,3-f]indole-2,6(1H,3H)-dione (8) (50.0 mg, 0.06 mmol), 1,5-bis(2-decyltetradecyl)-1,5-dihydropyrrolo[2,3-f]indole-2,3,6,7-tetraone (9) (51.6 mg, 0.06 mmol), p-toluene sulfonic acid (3.3 mg, 0.02 mmol) and 4 Å molecular sieves. The vial was sealed and dry toluene (2 ml), already degassed for 30 minutes was injected into the vial. The reaction was heated at 120° C. for 21 hours followed by 10 hours at 180° C. in the dark. The reaction mixture changed colour from blue to red/brown to dark purple over the polymerization period. The crude polymer was precipitated in methanol and purified by Soxhlet extraction with methanol, acetone, and hexane. The hexane fraction was collected and reduced under vacuum and the polymer precipitated into methanol. The polymer was filtered and dried. Yield of P1: 83 mg, 82% dark purple solid. ¹H NMR (400 MHz, Chloroform-d) δ 9.30 (d, J=8.2 Hz, 2H), 8.93 (s, 2H), 7.11 (d, J=8.2 Hz, 2H), 3.75 (dd, J=13.6, 7.3 Hz, 8H), 2.02 (dt, J=12.8, 6.1 Hz, 4H), 1.66-1.12 (m, 150H), 0.91-0.79 (m, J=3.7 Hz, 24H).

M_(n)=18 400 g/mol, M_(w)=29 900 g/mol, PDI=1.6

Example 12 Fabrication and Electrical Characterization of an Organic Field-Effect Transistor (OFET) Based on Compound P1 Preparation of Back-Contact, Top-Gate FETs

Compound P1 is dissolved at a concentration of 0.75 wt % in toluene. The transistors have been fabricated on a PET-substrate with lithographically prepatterned gold contacts, serving as Source and Drain contact of the FET. Before the deposition of the semiconductor, the substrate been immersed in a 1 wt % solution of 4-methoxybenzenethiol in ethanol for 2 minutes. Afterwards the substrate has been rinsed with ethanol and blown dry using nitrogen. Next, the semiconductor formulation was applied by spin coating (1,000 rpm, 15 seconds). After the coating is completed, the substrate is immediately transferred onto a preheated hotplate and heated for 30 s at 90° C. Next the gate dielectric layer consisting of Cytop CTL-809 M is spincoated on top of the organic semiconductor (1250 rpm, 30 s). After Spincoating, the substrate is again transferred to the hotplate and annealed for another 5 Min at 90° C. The thickness of the dielectric layer is 500 nm measured by profilometer. Finally 50 nm thick shadow-mask patterend gold gate electrodes are deposited by vacuum evaporation to complete FETs in the BCTG-configuration.

Electrical Characterization

The devices obtained are showing n-type characteristics. The mobility is calculated from the root representation of the transfer characteristic curve (solid grey curve) calculated in the saturation region. The slope m is determined from the dashed black line in FIG. 1. The dashed black line in FIG. 1 is fitted to a region of the root representation of the current characteristic ID such that a good correlation to the linear slope of the root representation is obtained. The threshold voltage U_(Th) can be taken from the intersection of black dashed line in FIG. 1 with the X-axis portion (V_(GS)).

In order to calculate the electrical properties of the OFET, the following equations are employed:

$\begin{matrix} {\mu = \frac{m^{2}*2L}{C_{G}*W}} & {C_{G} = {ɛ_{0}*ɛ_{r}\frac{1}{d}}} & {U_{Th} = {{- 1}*\frac{m}{b}}} & {{{ON}\text{/}{OFF}} = \frac{I_{D}\mspace{14mu} \max}{I_{D}\mspace{14mu} \min}} \end{matrix}$

where ε₀ is the vacuum permittivity of 8.85×10⁻¹² As/Vm, ε_(r)=2.1 for Cytop, the thickness of the dielectric d=500 nm, and W/L=25.

The following mobility has been calculated for the respective compound:

Field-effect mobility Threshold voltage ON/OFF Compound μ [cm²/Vs] U_(TH) [V] ratio P1 9E−5 15 2E2

FIG. 1 shows a representative transfer characteristics of a FET fabricated from compound P1 with V_(GS)=−10 V to +30 V at 0.5V step size with V_(DS)=+30V. Drain current (black solid curve), Gate current (dotted grey curve), Square root of drain current (grey solid curve), and fitted slope of square root (dashed black curve).

Example 13

Compound 12 was synthesized according to the reference (J. Mater. Chem. A. 2016, 4, 6940-6945), which was used as crude product without purification.

The crude bisisatin 12 (300 mg, 1.13 mmol) and dry K₂CO₃ (660 mg, 4.78 mmol) and the alkyliodide [1639798-42-7] (2.2 g, 3.26 mmol) were dissolved in 10 mL of dry DMF. The reaction mixture was heated to 100° C. for 4 hours. After cooling down, the reaction mixture was poured over 20 mL H₂O. The aqueous layer was extracted with CHCl₃. The organic layers were dried over MgSO₄ and concentrated to yield the crude reside. The crude product was purified by column chromatography on silica gel (CHCl₃:hexane: 2:1) to get the compound 13. Recrystallization with dichloromethane and methanol, collected and dried in vacuum. Total yield: 230 mg (15%). ¹H NMR (400 MHz, CDCl3, rt): δ=7.99 (d, J=8.7 Hz, 2H), 7.67 (d, J=8.6 Hz, 2H), 4.28-4.24 (m, 4H), 1.79-1.74 (m, 4H), 1.59-1.12 (M, 152H), 0.91-0.88 (m, 12H). ¹³C NMR (100 MHz, CDCl3, rt): δ=182.76, 158.96, 152.24, 127.21, 120.08, 119.64, 116.27, 42.12, 35.90, 33.46, 33.16, 31.94, 29.99, 29.72, 29.68, 29.37, 26.63, 22.70, 14.12. Calculated: C92H162N2O. 1359.25, Found: [M+H]: 1360.6.

Example 14 Polymerization to Give pDPID P9

Compound 14 was synthesized according to ref: J. Am. Chem. Soc. 2014, 136, 2135-2141. Polymer P9: To a vial was added 13 (71.82 mg, 0.053 mmol, 1 equiv) and bisoxindole 14 (10.04 mg, 0.053 mmol, 1 equiv), PTSA (2 mg). The tube was sealed and flushed with Argon, and then 0.5 ml degassed toluene was added. The mixture was thoroughly degassed under Argon for half an hour, and then the argon inlet was removed. The vial was heated at 120° C. for 3 days. After cooling to RT, the polymer was precipitated into methanol, and filtered through a Soxhlet thimble. The polymer was extracted using Soxhlet apparatus with methanol, acetone, hexane and chloroform. The hexane and chloroform fractions were concentrated and precipitated into methanol. The precipitates were filtered and dried under vacuum to afford P9 as a dark solid (59 mg, 73%). GPC (chlorobenzene, 80° C.): Mn: 25.2 KDa, Mw: 44.3 KDa, PDI=1.76. ¹H-NMR (TCE-d₂, 403 K, 400 Hz): δ=9.04 (broad), 7.76 (broad), 4.34 (broad), 2.18-0.85 (m).

Example 15 Polymerization to Give pDPID P10

Compound 15 was synthesized according to the ref: Chem. Commun., 2015, 51, 13515. Polymer P10: To a vial was added 13 (52.78 mg, 0.039 mmol, 1 equiv.) and bisoxindole 15 (9.32 mg, 0.039 mmol, 1 equiv), PTSA (2 mg). The tube was sealed and flushed with Argon, and then 0.5 ml degassed toluene was added. The mixture was thoroughly degassed under Argon for half an hour, and then the argon inlet was removed. The vial was heated at 120° C. for 3 days. After cooling to RT, the polymer was precipitated into methanol, and filtered through a Soxhlet thimble. The polymer was extracted using Soxhlet apparatus with methanol, acetone, hexane and chloroform. The hexane and chloroform fractions were concentrated and precipitated into methanol. The precipitates were filtered and dried under vacuum to afford P10 as a dark solid (47 mg, 77%). GPC (chlorobenzene, 80° C.): Mn: 10.5 k, Mw: 15.7 K, PDI: 1.49. ¹HNMR (TCE-d2, 403 K, 400 Hz): δ=9.33 (d), 9.20 (d), 9.10 (d), 8.05-7.94 (m), 7.71 (d), 7.64 (d), 4.41-4.27 (m), 1.98-1.82 (m), 1.38-0.94 (m).

Example 16 Polymerization to Give pDPID P11

Compound 16 was synthesized according to the ref: Organic Electronics 37 (2016) 190-196. Polymer P11: To a vial was added 13 (80.95 mg, 0.0595 mmol, 1 equiv.) and bisoxindole 16 (24.39 mg, 0.04 mmol, 1 equiv), PTSA (4 mg). The tube was sealed and flushed with Argon, and then 0.7 ml degassed toluene was added. The mixture was thoroughly degassed under Argon for half an hour, and then the argon inlet was removed. The vial was heated at 120° C. for 3 days. After cooling to RT, the polymer was precipitated into methanol, and filtered through a Soxhlet thimble. The polymer was extracted using Soxhlet apparatus with methanol, acetone, hexane and chloroform. The hexane and chloroform fractions were concentrated and precipitated into methanol. The precipitates were filtered and dried under vacuum to afford P11 as a dark solid (65 mg, 70%). GPC (chlorobenzene, 80° C.): Mn=21.1 K, Mw=31.2 K, PDI=1.48. ¹HNMR (TCE-d₂, 403 K, 400 Hz): δ=8.71 (broad), 8.01 (broad), 7.57 (broad), 4.33 (broad), 2.12-0.76 (m).

Example 17

Compound 17 was synthesized according to compound 13 in example 13 with [1044598-79-9] as alkyl iodide instead of [1639798-42-7].

Example 18 Polymerization to Give pDPID P12

To a microwave vial was added the respective bisisatin 17 (0.1 mmol, 1.0 e.q.) and then sealed. The sealed vial was degassed via vacuum and then purged with argon for three cycles. Anhydrous degassed toluene was added under argon and then tris(diethylamino)phosphine P(NEt₂)₃ (0.22 mmol, 2.2 e.q.) was added to the mixture at room temperature under bubbling of argon. The mixture turned dark green and then the temperature increased to 100° C. After reaction for 3 hours, the reaction mixture turned dark purple and was then poured into methanol. The resulting polymeric precipitate was filtered via thimble and then purified by Soxhlet extraction in a sequence of methanol, hexane, ethyl acetate, and finally chloroform. The chloroform fraction was concentrated by rotary evaporation, suspended in methanol and filtered to afford the polymer as a metallic dark green solid. GPC (Chlorobenzene at 80° C.): M_(n)=20.2 kDa, M_(w)=72.5 kDa, PDI=3.59.

Example 19 Synthesis of Thieno[3,2-b]thiophene Bisisatin 23

Compound 18 was synthesized according to the literature: Adv. Mater. 28, 6921-6925 (2016).

Synthesis of Compound 19:

To a mixture of dimethyl thieno[3,2-b]thiophene-3,6-dicarboxylate (18) (0.77 g, 3.0 mmol, 1.0 e.q.) in ethanol/tetrahydrofuran/water (50 mL/50 mL/5 mL) was added sodium hydroxide (1.5 g, 37.5 mmol, 12.5 e.q.). After the reaction mixture was refluxed overnight, the solvent was evaporated under vacuum to about half of its original volume. Water (50 mL) was added to the mixture and the solution was treated with concentrated hydrochloric acid until white precipitates formed. The precipitate was filtered and then washed with water to give thieno[3,2-b]thiophene-3,6-dicarboxylic acid (19) as a white solid which was dried in a vacuum oven and then used in the next step without further purifications (0.61 g, 2.67 mmol, 89% yield).

Synthesis of Compound 20:

Thieno[3,2-b]thiophene-3,6-dicarboxylic acid (19) (0.55 g, 2.4 mmol, 1.0 e.q.), diphenylphosphoryl azide DPPA (0.56 mL, 2.6 mmol, 1.08 e.q.) and triethylamine (0.36 mL, 2.6 mmol, 1.08 e.q.) were combined in anhydrous tert-butanol (4.5 mL) and the resulting mixture was heated to reflux. After reaction overnight, the solution was cooled and then concentrated in vacuum to remove solvent. The residue was taken up in diethyl ether and washed with 5% aqueous citric acid, water and brine, dried with MgSO₄, and concentrated. The crude product was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:4) as the eluent to give di-tert-butyl thieno[3,2-b]thiophene-3,6-diyldicarbamate (20) as a light brown solid. (0.60 g, 1.61 mmol, 67% yield). ¹H NMR (400 MHz, CDCl₃) δ 7.38 (s, 2H), 6.60 (s, 2H), 1.57 (s, 18H).

Synthesis of Compound 21:

Di-tert-butyl thieno[3,2-b]thiophene-3,6-diyldicarbamate (20) (0.93 g, 2.5 mmol, 1.0 e.q.) was dissolved in DMF (25 mL) and cooled to 0° C. Sodium hydride (0.40 g, 60% dispersion in mineral oil, 10.0 mmol, 4.0 e.q.) was added and the solution was stirred at room temperature for 1 hour. 7-(bromomethyl)pentadecane (2.29 g, 7.5 mmol, 3.0 e.q.) was added to the mixture and the solution was stirred at 80° C. for 3 hours. After the solution cooled to room temperature, the mixture was poured into iced water, followed by extraction with ethyl acetate for three times. The organic layers were combined, washed with water, brine and then dried over MgSO₄, concentrated. The resulting brown oil was purified via silica gel column chromatography with dichloromethane/petroleum ether (1:1) as the eluent to give di-tert-butyl thieno[3,2-b]thiophene-3,6-diylbis((2-hexyldecyl)carbamate) as a light brown oil (21) (1.64 g, 2.0 mmol, 80% yield). ¹H NMR (400 MHz, CDCl₃) δ 7.04 (s, 2H), 3.62 (d, J=7.2 Hz, 4H), 1.58-1.48 (m, 2H), 1.34-1.11 (m, 48H), 0.87 (q, J=6.8 Hz, 12H). ¹³C NMR (101 MHz, CDCl₃) δ 154.13, 134.76, 133.70, 119.18, 80.64, 53.38, 36.93, 31.90, 31.77, 31.21, 30.03, 29.68, 29.52, 29.29, 28.15, 26.31, 26.25, 22.66, 22.62, 14.08.

Synthesis of Compound 22:

Di-tert-butylthieno[3,2-b]thiophene-3,6-diylbis((2-hexyldecyl)carbamate) (21) (1.64 g, 2.0 mmol, 1.0 e.q.) was dissolved in dichloromethane (20 mL) and cooled to 0° C. Trifluoroacetic acid (2.7 mL) was added and the reaction mixture was allowed to warm to room temperature and stirred for overnight. The mixture was poured into water, washed with sodium bicarbonate, brine, dried over MgSO₄ and then concentrated to afford N³,N⁶-bis(2-hexyldecyl)thieno[3,2-b]thiophene-3,6-diamine (22) a light brown oil. The product is unstable in air and used immediately without further purifications in the next step (1.1 g, 1.78 mmol, 89% yield). ¹H NMR (400 MHz, CDCl₃) δ 5.97 (s, 2H), 3.53 (s, 2H), 3.10 (d, J=6.1 Hz, 4H), 1.72-1.63 (m, 2H), 1.50-1.16 (m, 48H), 0.91 (t, J=6.6 Hz, 12H).

Synthesis of Compound 23:

N³,N⁶-bis(2-hexyldecyl)thieno[3,2-b]thiophene-3,6-diamine (22) (1.1 g, 1.78 mmol, 1.0 e.q.) in anhydrous dichloromethane (5 mL) was added dropwise to a stirring solution of oxalyl chloride (0.39 mL, 4.63 mmol, 2.6 e.q.) in anhydrous dichloromethane (10 mL) at 0° C. The mixture was allowed to warm to room temperature and stirred for one hour. Triethylamine (2.23 mL, 16.02 mmol, 9.0 e.q.) in anhydrous dichloromethane (5 mL) was added dropwise at room temperature and the solution was stirred for overnight. The mixture was poured into water and then extracted with dichloromethane for three times. The organic layers were combined, washed with water, brine and then dried over MgSO₄, concentrated. The crude product was purified via silica gel column chromatography with dichloromethane/petroleum ether (3:2) as the eluent and then recrystallized with dichloromethane/methanol to the product (23) as a purple solid. ¹H NMR (400 MHz, CDCl₃) δ 3.70 (d, J=7.7 Hz, 4H), 1.87 (q, J=6.4 Hz, 2H), 1.47-1.20 (m, 48H), 0.93-0.86 (m, 12H). 13C NMR (101 MHz, CDCl₃) δ 173.02, 160.00, 157.06, 134.45, 116.98, 47.23, 38.99, 31.86, 31.73, 31.28, 29.97, 29.64, 29.49, 29.28, 26.24, 26.19, 22.67, 22.64, 14.13, 14.09.

Example 20 Polymerization to Give pDPID P14

Polymer P14 was synthesized from compound 23 according to the procedure for polymer P12 in example 18. 

1-20. (canceled) 21: A polymer comprising a structure of formula (II′)

wherein Q^(a), Q^(b), Q^(c) and Q^(d) are independently O, S or an NR¹ group, wherein Ar and Ar′ are independently selected from the group consisting of

wherein each Y, Y′, Y″ and Y* is independently O, S, an NR^(1a) group, Se, or Te, and wherein each R^(W) is independently H, a C₁₋₃₀-alkyl group, a C₁₋₃₀-alkoxy group, or a moiety

wherein R^(s1), R^(s2) and R^(s3) are independently H, a C₁₋₂₀-alkyl group, a C₂₋₂₀-alkenyl group, or a phenyl group, wherein Ar or Ar′ is bound via the single bonds

and

to the moieties

wherein Q is Q^(a), Q^(b), Q^(c) or Q^(d), wherein Ar and/or Ar′ optionally comprise a substituent R², wherein each R¹ and R^(1a) is independently selected from the group consisting of H, a C₁₋₁₀₀-alkyl group, a C₂₋₁₀₀-alkenyl group, a C₂₋₁₀₀-alkynyl group, a C₅₋₁₂-cycloalkyl group, a C₆₋₁₈-aryl group, a 5 to 20 membered heteroaryl group, a C(O)—C₁₋₁₀₀-alkyl group, a C(O)—C₅₋₁₂-cycloalkyl group and a C(O)—OC₁₋₁₀₀-alkyl group, wherein the C₁₋₁₀₀-alkyl group, the C₂₋₁₀₀-alkenyl group and the C₂₋₁₀₀-alkynyl group optionally comprise one to forty substituents independently selected from the group consisting of a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an OR^(a) group, an OC(O)—R^(a) group, a C(O)—OR^(a) group, a C(O)—R^(a) group, an NR^(a)R^(b) group, an NR^(a)—C(O)R^(b) group, a C(O)—NR^(a)R^(b) group, an N[C(O)R^(a)][C(O)R^(b)] group, an SR^(a) group, an Si(R^(Sia))(R^(Sib))(R^(Sic)) group, an —O—Si(R^(Sia))(R^(Sib))(R^(Sic)) group, a halogen, CN, and NO₂, wherein at least two CH₂-groups, but not adjacent CH₂-groups, of the C₁₋₁₀₀-alkyl group, the C₂₋₁₀₀-alkenyl group and/or the C₂₋₁₀₀-alkynyl group can be replaced by O or S, wherein the C₅₋₁₂-cycloalkyl group optionally comprises one to six substituents independently selected from the group consisting of a C₁₋₆₀-alkyl group, a C₂₋₆₀-alkenyl group, a C₂₋₆₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an OR^(a) group, an OC(O)—R^(a) group, a C(O)—OR^(a) group, a C(O)—R^(a) group, an NR^(a)R^(b) group, an NR^(a)—C(O)R^(b) group, a C(O)—NR^(a)R^(b) group, an N[C(O)R^(a)][C(O)R^(b)] group, an SR^(a) group, an Si(R^(Sia))(R^(Sib))(R^(Sic)) group, an —O—Si(R^(Sia))(R^(Sib))(R^(Sic)) group, a halogen, CN, and NO₂, wherein one or two CH₂-groups, but not adjacent CH₂-groups, of the C₅₋₁₂-cycloalkyl group can be replaced by O, S, OC(O), CO, an NR^(a) group or an NR^(a)—CO group, and wherein the C₆₋₁₈-aryl group and the 5 to 20 membered heteroaryl group optionally comprise one to six substituents independently selected from the group consisting of a C₁₋₆₀-alkyl group, a C₂₋₆₀-alkenyl group, a C₂₋₆₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an OR^(a) group, an OC(O)—R^(a) group, a C(O)—OR^(a) group, a C(O)—R^(a) group, an NR^(a)R^(b) group, an NR^(a)—C(O)R^(b) group, a C(O)—NR^(a)R^(b) group, an N[C(O)R^(a)][C(O)R^(b)] group, an SR^(a) group, an Si(R^(Sia))(R^(Sib))(R^(Sic)) group, an —O—Si(R^(Sia))(R^(Sib))(R^(Sic)) group, a halogen, CN, and NO₂, wherein R^(a) and R^(b) are independently selected from the group consisting of H, a C₁₋₆₀-alkyl group, a C₂₋₆₀-alkenyl group, a C₂₋₆₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group and a 5 to 14 membered heteroaryl group, and wherein R^(Sia), R^(Sib) and R^(Sic) are independently selected from the group consisting of H, a C₁₋₆₀-alkyl group, a C₂₋₆₀-alkenyl group, a C₂₋₆₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an O—C₁₋₆₀-alkyl group, an O—C₂₋₆₀-alkenyl group, an O—C₂₋₆₀-alkynyl group, an O—C₅₋₈-cycloalkyl group, an O—C₆₋₁₄-aryl group, an O-5 to 14 membered heteroaryl group, an —[O—SiR^(Sid)R^(Sie)]_(o)—R^(Sif) group, an NR⁵R⁶ group, a halogen and an O—C(O)—R⁵ group, wherein o is an integer from 1 to 50, wherein R^(Sid), R^(Sie), R^(Sif) are independently selected from the group consisting of H, a C₁₋₆₀-alkyl group, a C₂₋₆₀-alkenyl group, a C₂₋₆₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an O—C₁₋₆₀-alkyl group, an O—C₂₋₆₀-alkenyl group, an O—C₂₋₆₀-alkynyl group, an O—C₅₋₈-cycloalkyl group, an O—C₆₋₁₄-aryl group, an O-5 to 14 membered heteroaryl group, an —[O—SiR^(Sig)R^(Sih)]_(p)—R^(Sii) group, an NR⁵⁰R⁶⁰ group, a halogen and an O—C(O)—R⁵⁰ group,  wherein p is an integer from 1 to 50, and  wherein R^(Sig) R^(Sih), R^(Sii) are independently selected from the group consisting of H, a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an O—C₁₋₃₀-alkyl group, an O—C₂₋₃₀-alkenyl group, an O—C₂₋₃₀-alkynyl group, an O—C₅₋₆-cycloalkyl group, an O—C₆₋₁₀-aryl group, an O-5 to 10 membered heteroaryl group, an O—Si(CH₃)₃ group, an NR⁵⁰⁰R⁶⁰⁰ group, a halogen and an O—C(O)—R⁵⁰⁰ group, and wherein R⁵, R⁶, R⁵⁰, R⁶⁰, R⁵⁰⁰ and R⁶⁰⁰ are independently selected from the group consisting of H, a C₁₋₆₀-alkyl group, a C₂₋₆₀-alkenyl group, a C₂₋₆₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, and a 5 to 14 membered heteroaryl group,  wherein the C₁₋₆₀-alkyl group, the C₂₋₆₀-alkenyl group and the C₂₋₆₀-alkynyl group optionally comprise one to twenty substituents selected from the group consisting of a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, an OR^(c) group, an OC(O)—R^(c) group, a C(O)—OR^(c) group, a C(O)—R^(c) group, an NR^(c)R^(d) group, an NR^(c)—C(O)R^(d) group, a C(O)—NR^(c)R^(d) group, an N[C(O)R^(c)][C(O)R^(d)] group, an SR^(c) group, an Si(R^(Sij))(R^(Sik))(R^(Sil)) group, an —O—Si(R^(Sij))(R^(Sik))(R^(Sil)) group, a halogen, CN, and NO₂,  wherein at least two CH₂-groups, but not adjacent CH₂-groups, of the C₁₋₆₀-alkyl group, the C₂₋₆₀-alkenyl group and/or the C₂₋₆₀-alkynyl group can be replaced by O or S,  wherein the C₅₋₈-cycloalkyl group optionally comprises one to five substituents selected from the group consisting of a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, an OR group, an OC(O)—R^(c) group, a C(O)—OR^(c) group, an C(O)—R^(c) group, an NR^(c)R^(d) group, an NR^(c)—C(O)R^(d) group, a C(O)—NR^(c)R^(d) group, an N[C(O)R^(c)][C(O)R^(d)] group, an SR^(c) group, an Si(R^(Sij))(R^(Sik))(R^(Sil)) group, an —O—Si(R^(Sij))(R^(Sik))(R^(Sil)) group, a halogen, CN, and NO₂,  wherein one or two CH₂-groups, but not adjacent CH₂-groups, of the C₅₋₈-cycloalkyl group can be replaced by O, S, OC(O), CO, an NR group or an NR^(c)—CO group, and  wherein the C₆₋₁₄-aryl group and the 5 to 14 membered heteroaryl group optionally comprise one to five substituents independently selected from the group consisting of a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, an OR group, an OC(O)—R^(c) group, a C(O)—OR^(c) group, a C(O)—R^(c) group, an NR^(c)R^(d) group, an NR^(c)—C(O)R^(d) group, a C(O)—NR^(c)R^(d) group, an N[C(O)R^(c)][C(O)R^(d)] group, an SR^(c) group, an Si(R^(Sij))(R^(Sik))(R^(Sil)) group, an —O—Si(R^(Sij))(R^(Sik))(R^(Sil)) group, a halogen, CN and NO₂,  wherein R^(c) and R^(d) are independently selected from the group consisting of H, a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group and a C₂₋₃₀-alkynyl group,  wherein R^(Sij), R^(Sik) and R^(Sil) are independently selected from the group consisting of H, a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an O—C₁₋₃₀-alkyl group, an O—C₂₋₃₀-alkenyl group, an OC₂₋₃₀-alkynyl group, an O—C₅₋₆-cycloalkyl group, an O—C₆₋₁₀-aryl group, an O-5 to 10 membered heteroaryl group, an —[O—SiR^(Sim)R^(Sin)]_(q)—R^(Sio) group, an NR⁷R⁸ group, a halogen, and an O—C(O)—R⁷ group,  wherein q is an integer from 1 to 50,  wherein R^(Sim), R^(Sin), R^(Sio) are independently selected from the group consisting of H, a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an O—C₁₋₃₀-alkyl group, an O—C₂₋₃₀-alkenyl group, an O—C₂₋₃₀-alkynyl group, an O—C₅₋₆-cycloalkyl group, an OC₆₋₁₀-aryl group, an O-5 to 10 membered heteroaryl group, an —[O—SiR^(Sip)R^(Siq)]_(r)—R^(Sir) group, an NR⁷⁰R⁸⁰ group, a halogen, and an O—C(O)—R⁷⁰ group,  wherein r is an integer from 1 to 50, and  wherein R^(Sip), R^(Siq), R^(Sir) are independently selected from the group consisting of H, a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an O—C₁₋₃₀-alkyl group, an OC₂₋₃₀-alkenyl group, an O—C₂₋₃₀-alkynyl group, an O—C₅₋₆-cycloalkyl group, an O—C₆₋₁₀-aryl group, an O-5 to 10 membered heteroaryl group, an O—Si(CH₃)₃ group, an NR⁷⁰⁰R⁸⁰⁰ group, a halogen and an O—C(O)—R⁷⁰⁰ group, and  wherein R⁷, R⁸, R⁷⁰, R⁸⁰, R⁷⁰⁰ and R⁸⁰⁰ are independently selected from the group consisting of H, a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, and a 5 to 10 membered heteroaryl group, and  wherein the C₁₋₃₀-alkyl group, the C₂₋₃₀-alkenyl group and the C₂₋₃₀-alkynyl group optionally comprise one to ten substituents selected from the group consisting of a halogen, CN and NO₂, wherein each R² is selected from the group consisting of a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₁₂-cycloalkyl group, a C₆₋₁₈-aryl group, a 5 to 20 membered heteroaryl group, an OR²¹ group, an OC(O)—R²¹ group, a C(O)—OR²¹ group, a C(O)—R²¹ group, an NR²¹R²² group, an NR²¹—C(O)R²² group, a C(O)—NR²¹R²² group, an N[C(O)R²¹][C(O)R²²] group, an SR²¹ group, a halogen, CN, an SiR^(Sis)R^(Sit)R^(Sin) group and OH, wherein R²¹ and R²² and are independently selected from the group consisting of H, a C₁₋₃₀-alkyl group, a C₂₋₃₀-alkenyl group, a C₂₋₃₀-alkynyl group, a C₅₋₁₂-cycloalkyl group, a C₆₋₁₈-aryl group and a 5 to 20 membered heteroaryl group, wherein the C₁₋₃₀-alkyl group, the C₂₋₃₀-alkenyl group and the C₂₋₃₀-alkynyl group optionally comprise one to ten substituents independently selected from the group consisting of a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an OR^(e) group, an OC(O)—R^(e) group, a C(O)—OR^(e) group, a C(O)—R^(e) group, an NR^(e)R^(f) group, an NR^(e)—C(O)R^(f) group, a C(O)—NR^(e)R^(f) group, an N[C(O)R^(e)][C(O)R^(f)] group, an SR^(e) group, a halogen, CN, an SiR^(Sis)R^(Sit)R^(Siu) group and NO₂, wherein at least two CH₂-groups, but not adjacent CH₂-groups, of the C₁₋₃₀-alkyl group, the C₂₋₃₀-alkenyl group and/or the C₂₋₃₀-alkynyl group can be replaced by O or S, wherein the C₅₋₁₂-cycloalkyl optionally comprises one to six substituents independently selected from the group consisting of a C₁₋₂₀-alkyl group, a C₂₋₂₀-alkenyl group, a C₂₋₂₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an OR^(e) group, an OC(O)—R^(e) group, a C(O)—OR^(e) group, a C(O)—R^(e) group, an NR^(e)R^(f) group, an NR^(e)—C(O)R^(f) group, a C(O)—NR^(e)R^(f) group, an N[C(O)R^(e)][C(O)R^(f)] group, an SR^(e) group, a halogen, CN, an SiR^(Sis)R^(Sit)R^(Siu) group and NO₂, wherein one or two CH₂-groups, but not adjacent CH₂-groups, of the C₅₋₁₂-cycloalkyl group can be replaced by O, S, OC(O), CO, an NR^(e) group or an NR^(e)—CO group, and wherein the C₆₋₁₈-aryl group and the 5 to 20 membered heteroaryl group optionally comprise one to six substituents independently selected from the group consisting of a C₁₋₂₀-alkyl group, a C₂₋₂₀-alkenyl group, a C₂₋₂₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, a 5 to 14 membered heteroaryl group, an OR^(e) group, an OC(O)—R^(e) group, a C(O)—OR^(e) group, a C(O)—R^(e) group, an NR^(e)R^(f) group, an NR^(e)—C(O)R^(f) group, a C(O)—NR^(e)R^(f) group, an N[C(O)R^(e)][C(O)R^(f)] group, an SR^(e) group, a halogen, CN, an SiR^(Sis)R^(Sit)R^(Siu) group and NO₂, wherein R^(Sis), R^(Sit) and R^(Siu) are independently selected from the group consisting of H, a C₁₋₂₀-alkyl group, a C₂₋₂₀-alkenyl group, a C₂₋₂₀-alkynyl group, a C₅₋₆-cycloalkyl group, a phenyl group and an O—Si(CH₃)₃ group, and wherein R^(e) and R^(f) are independently selected from the group consisting of H, a C₁₋₂₀-alkyl group, a C₂₋₂₀-alkenyl group, a C₂₋₂₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, and a 5 to 14 membered heteroaryl group, wherein the C₁₋₂₀-alkyl group, the C₂₋₂₀-alkenyl group and the C₂₋₂₀-alkynyl group optionally comprise one to five substituents selected from the group consisting of a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an OR^(g) group, an OC(O)—R^(g) group, a C(O)—OR^(g) group, a C(O)—R^(g) group, an NR^(g)R^(h) group, an NR^(g)—C(O)R^(h) group, a C(O)—NR^(g)R^(h) group, an N[C(O)R^(g)][C(O)R^(h)] group, an SR^(g) group, a halogen, CN, and NO₂, wherein the C₅₋₈-cycloalkyl group optionally comprises one to five substituents selected from the group consisting of a C₁₋₁₀-alkyl group, a C₂₋₁₀-alkenyl group, a C₂₋₁₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an OR^(g) group, an OC(O)—R^(g) group, a C(O)—OR group, a C(O)—R group, an NR^(g)R^(h) group, an NR^(g)—C(O)R^(h) group, a C(O)—NR^(g)R^(h) group, an N[C(O)R^(g)][C(O)R^(h)] group, an SR^(g) group, a halogen, CN, and NO₂, and wherein the C₆₋₁₄-aryl group and the 5 to 14 membered heteroaryl group optionally comprise one to five substituents independently selected from the group consisting of a C₁₋₁₀-alkyl group, a C₂₋₁₀-alkenyl group, a C₂₋₁₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an OR^(g) group, an OC(O)—R group, a C(O)—OR^(g) group, a C(O)—R group, an NR^(g)R^(h) group, an NR^(g)—C(O)R^(h) group, a C(O)—NR^(g)R^(h) group, an N[C(O)R^(g)][C(O)R^(h)] group, an SR^(g) group, a halogen, CN, and NO₂,  wherein R^(g) and R^(h) are independently selected from the group consisting of H, a C₁₋₁₀-alkyl group, a C₂₋₁₀-alkenyl group and a C₂₋₁₀-alkynyl group,  wherein the C₁₋₁₀-alkyl group, the C₂₋₁₀-alkenyl group and the C₂₋₁₀-alkynyl group optionally comprise one to five substituents selected from the group consisting of a halogen, CN and NO₂, wherein each R¹⁰⁰ and R¹⁰¹ is independently selected from the group consisting of H, a C₁₋₂₀-alkyl group, a C₂₋₂₀-alkenyl group, a C₂₋₂₀-alkynyl group, a C₅₋₈-cycloalkyl group, a C₆₋₁₄-aryl group, and a 5 to 14 membered heteroaryl group; or wherein R¹⁰⁰ and R¹⁰¹, if attached to a same atom, together with the same atom, form a 5 to 12 membered ring system, wherein the C₁₋₂₀-alkyl group, the C₂₋₂₀-alkenyl group and the C₂₋₂₀-alkynyl group optionally comprise one to five substituents selected from the group consisting of a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an OR^(q) group, an OC(O)—R^(q) group, a C(O)—OR^(q) group, a C(O)—R^(q) group, an NR^(q)R^(r) group, an NR^(q)C(O)R^(r) group, a C(O)—NR^(g)R^(r) group, an N[C(O)R^(q)][C(O)R^(r)] group, an SR^(q) group, a halogen, CN, and NO₂, wherein the C₅₋₈-cycloalkyl group optionally comprises one to five substituents selected from the group consisting of a C₁₋₁₀-alkyl group, a C₂₋₁₀-alkenyl group, a C₂₋₁₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an OR^(q) group, an OC(O)—R^(q) group, a C(O)—OR^(q) group, a C(O)—R^(q) group, an NR^(q)R^(r) group, an NR^(q)—C(O)R^(r) group, a C(O)—NR^(q)R^(r) group, an N[C(O)R^(q)][C(O)R^(r]) group, an SR^(q) group, a halogen, CN, and NO₂, wherein the C₆₋₁₄-aryl group and the 5 to 14 membered heteroaryl group optionally comprise one to five substituents independently selected from the group consisting of a C₁₋₁₀-alkyl group, a C₂₋₁₀-alkenyl group, a C₂₋₁₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an OR^(q) group, an OC(O)—R^(g) group, a C(O)—OR^(g) group, a C(O)—R^(g) group, an NR^(q)R^(r) group, an NR^(q)—C(O)R^(r) group, a C(O)—NR^(q)R^(r) group, an N[C(O)R^(q)][C(O)R^(r)] group, a SR^(q) group, a halogen, CN, and NO₂, and wherein the 5 to 12 membered ring system optionally comprises one to five substituents selected from the group consisting of a C₁₋₁₀-alkyl group, a C₂₋₁₀-alkenyl group, a C₂₋₁₀-alkynyl group, a C₅₋₆-cycloalkyl group, a C₆₋₁₀-aryl group, a 5 to 10 membered heteroaryl group, an OR^(q) group, an OC(O)—R^(g) group, a C(O)—OR^(g) group, a C(O)—R^(g) group, an NR^(q)R^(r) group, an NR^(q)—C(O)R^(r) group, a C(O)—NR^(q)R^(r) group, an N[C(O)R^(q)][C(O)R^(r)] group, an SR^(q) group, a halogen, CN, and NO₂, wherein R^(q) and R^(r) are independently selected from the group consisting of H, a C₁₋₁₀alkyl group, a C₂₋₁₀-alkenyl group and a C₂₋₁₀-alkynyl group,  wherein the C₁₋₁₀-alkyl group, the C₂₋₁₀-alkenyl group and the C₂₋₁₀-alkynyl group optionally comprise one to five substituents selected from the group consisting of a halogen, CN and NO₂, and wherein n is in a range from 3 to
 1000. 22: The polymer of claim 21, wherein Ar and Ar′ are independently selected from the group consisting of

23: The polymer of claim 21, wherein Ar and Ar′ are independently selected from the group consisting of

24: The polymer of claim 21, comprising a structure of formula 1′, 2′ or 3′

wherein R^(1b), R^(1c) and R^(1d) are independently defined as R^(1a). 25: A polymer comprising a structure of formula II″

wherein Q^(a), Q^(b), and Ar are as defined in claim 21, and wherein m is in a range from 3 to
 1000. 26: The polymer of claim 25, comprising a structure of formula 4′

wherein R^(1b) is independently defined as R^(1a), and wherein m is in a range from 3 to
 1000. 27: A process for preparing the polymer of claim 21, the process comprising condensing a tetraone A and a dione B:

wherein Q^(a), Q^(b), Q^(c), Q^(d), Ar and Ar′ are as defined in claim
 21. 28: The process of claim 27, wherein Q^(a) and Q^(b) are an NR¹ group, and wherein Q^(c) and Q^(d) are O or an NR¹ group. 29: A process for preparing the polymer of claim 25, the process comprising homopolymerizing a tetraone A:

30: An electronic device comprising the polymer of claim
 21. 31: The electronic device of claim 30, wherein the electronic device is an organic field effect transistor. 